Anzelc Madison, Druskovich Christina, Cusick Austin, Franklin Matthew
Department of Dermatology, Riverside Methodist OhioHealth Hospital, Columbus, Ohio, USA.
Michigan State University College of Human Medicine, Lansing, Michigan, USA.
Case Rep Dermatol Med. 2025 Mar 18;2025:8628105. doi: 10.1155/crdm/8628105. eCollection 2025.
Blastic plasmacytoid dendritic cell neoplasm (BPDCN) is a rare, highly aggressive CD4+ CD56+ hematopoietic malignancy. The cutaneous presentation is variable but often includes violaceous nodules. We present a rare case of BPDCN, which featured dermatological findings consisting of erythematous macules, petechiae, purpura, and a violaceous nodule. A skin biopsy and peripheral blood smear supported a diagnosis of BPDCN. With BPDCN favoring cutaneous involvement, we urge dermatologists to be aware of the possibility of a BPDCN diagnosis in patients who present with purpuric nodules and petechial skin findings, especially when it is not easily explainable by another pathology or medication.
母细胞性浆细胞样树突状细胞肿瘤(BPDCN)是一种罕见的、侵袭性很强的CD4+ CD56+造血系统恶性肿瘤。其皮肤表现多样,但常包括紫罗兰色结节。我们报告一例罕见的BPDCN病例,其皮肤表现为红斑、瘀点、紫癜和一个紫罗兰色结节。皮肤活检和外周血涂片支持BPDCN的诊断。鉴于BPDCN倾向于累及皮肤,我们敦促皮肤科医生意识到,对于出现紫癜性结节和瘀点性皮肤表现的患者,尤其是当这些表现无法轻易用其他病理或药物解释时,有BPDCN诊断的可能性。